Matsuzaki Shinya, Endo Masayuki, Ueda Yutaka, Mimura Kazuya, Kakigano Aiko, Egawa-Takata Tomomi, Kumasawa Keiichi, Yoshino Kiyoshi, Kimura Tadashi
Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
BMC Pregnancy Childbirth. 2017 Jun 14;17(1):188. doi: 10.1186/s12884-017-1380-y.
Sheehan's syndrome occurs because of severe postpartum hemorrhage causing ischemic pituitary necrosis. Sheehan's syndrome is a well-known condition that is generally diagnosed several years postpartum. However, acute Sheehan's syndrome is rare, and clinicians have little exposure to it. It can be life-threatening. There have been no reviews of acute Sheehan's syndrome and no reports of successful pregnancies after acute Sheehan's syndrome. We present such a case, and to understand this rare condition, we have reviewed and discussed the literature pertaining to it. An electronic search for acute Sheehan's syndrome in the literature from January 1990 and May 2014 was performed.
A 27-year-old woman had massive postpartum hemorrhage (approximately 5000 mL) at her first delivery due to atonic bleeding. She was transfused and treated with uterine embolization, which successfully stopped the bleeding. The postpartum period was uncomplicated through day 7 following the hemorrhage. However, on day 8, the patient had sudden onset of seizures and subsequently became comatose. Laboratory results revealed hypothyroidism, hypoglycemia, hypoprolactinemia, and adrenal insufficiency. Thus, the patient was diagnosed with acute Sheehan's syndrome. Following treatment with thyroxine and hydrocortisone, her condition improved, and she was discharged on day 24. Her next pregnancy was established 2 years after her first delivery. She required induction of ovulation for the next conception. The pregnancy, delivery, and postpartum period were uneventful. An electronic search of the literature yielded 21 cases of acute Sheehan's syndrome. Presenting signs varied, including adrenal insufficiency (12 cases), diabetes insipidus (4 cases), hypothyroidism (2 cases), and panhypopituitarism (3 cases), with a median time of presentation after delivery for each of those conditions being 7.9, 4, 18, and 9 days, respectively. Serial changes in magnetic resonance imaging were reported in some cases of acute Sheehan's syndrome.
Clinicians should be aware of the risk of acute Sheehan's syndrome after a massive postpartum hemorrhage in order to diagnose it accurately and treat it promptly.
席汉综合征是由于严重产后出血导致垂体缺血性坏死所致。席汉综合征是一种众所周知的疾病,通常在产后数年才被诊断出来。然而,急性席汉综合征很少见,临床医生对此接触甚少。它可能危及生命。目前尚无关于急性席汉综合征的综述,也没有急性席汉综合征后成功妊娠的报道。我们报告了这样一例病例,为了解这种罕见疾病,我们查阅并讨论了与之相关的文献。对1990年1月至2014年5月期间文献中关于急性席汉综合征的内容进行了电子检索。
一名27岁女性在首次分娩时因宫缩乏力性出血发生大量产后出血(约5000毫升)。她接受了输血治疗,并进行了子宫栓塞术,成功止血。产后第7天之前情况顺利。然而,在第8天,患者突然发作癫痫,随后昏迷。实验室检查结果显示甲状腺功能减退、低血糖、泌乳素水平低下和肾上腺功能不全。因此,该患者被诊断为急性席汉综合征。经甲状腺素和氢化可的松治疗后,她的病情有所改善,并于第24天出院。她在首次分娩2年后再次怀孕。下次受孕时她需要诱导排卵。此次妊娠、分娩及产后过程均顺利。对文献进行电子检索后发现21例急性席汉综合征病例。表现出的症状各不相同,包括肾上腺功能不全(12例)、尿崩症(4例)、甲状腺功能减退(2例)和全垂体功能减退(3例),这些情况在分娩后的中位发病时间分别为7.9天、4天、18天和9天。部分急性席汉综合征病例报告了磁共振成像的系列变化。
临床医生应意识到产后大出血后发生急性席汉综合征的风险,以便准确诊断并及时治疗。